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Dihydrostreptomycin

Product Name
Dihydrostreptomycin
CAS No.
128-46-1
Chemical Name
Dihydrostreptomycin
Synonyms
DHSM;dhms;abiocine;vibriomycin;DIHYDROSTREPTOMYCIN;dihydro-streptomyci;DihydroestreptoMycin Sulfate;Benzimidazole, 2-cyanomethyl;dihydrostreptomycine sulphate;Dihydrostreptomycin USP/EP/BP
CBNumber
CB9665040
Molecular Formula
C21H41N7O12
Formula Weight
583.59
MOL File
128-46-1.mol
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Dihydrostreptomycin Property

Melting point:
>300 °C
Boiling point:
641.09°C (rough estimate)
Density 
1.3963 (rough estimate)
refractive index 
1.6800 (estimate)
pka
pKa 7.8 (Uncertain)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Usbiological
Product number
D8035
Product name
Dihydrostreptomycin
Packaging
100g
Price
$72
Updated
2021/12/16
Usbiological
Product number
257286
Product name
Dihydrostreptomycin
Packaging
50g
Price
$470
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
CHM0014251
Product name
DIHYDROSTREPTOMYCIN
Purity
95.00%
Packaging
1G
Price
$1358.28
Updated
2021/12/16
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Dihydrostreptomycin Chemical Properties,Usage,Production

Description

Dihydrostreptomycin was first synthesized by Parke Davis Co. in 1946by the reduction of streptomycin. Naturally occurring dihydrostreptomycin was found in the culture broth of Streptomyces humidus by Takeda Chemicals Industries in 1957. Its hydrochloride or sulfate is more easily crystallized and more stable under alkaline conditions than streptomycin. Dihydrostreptomycin has been used for therapy of tuberculosis, but because it has a higher ototoxicity than streptomycin its use is now restricted to animal therapy.

Originator

Dihydrostrepto,MSD ,US,1948

Uses

Antibacterial.

Definition

ChEBI: Dihydrostreptomycin is a member of streptomycins.

Manufacturing Process

Dihydrostreptomycin sulfate may be prepared from streptomycin sulfate by catalytic hydrogenation (Merck, Pfizer, Cyanamid), electrolytic reduction (Schenley, Olin Mathieson), or by sodium borohydride reduction (Bristol), or by isolation from a fermentation process (Takeda).

brand name

Abocillin;Biostrep;Complexobiotico;Diapenin 3;Diapenin balsamico;Diarrestival;Didromycin;Didrothenate;Dihydrocidan sulfato;Dihydrostreptofar;Diidro-pantostrept;Distreptopab;Dreiciclina balsamica;Dst;Entera-strept;Estreptoluy;Estreptosirup;Helle-strep-forte;Hp 48;Mastigun;Mixtencillin;Retromyopen;Rocopenstrep;Sanstrepto;Solmycin;Solvo-strept;Streptoduocin;Veticar;Veycil-as.

Therapeutic Function

Antibiotic

World Health Organization (WHO)

Dihydrostreptomycin, a derivative of the aminoglycoside antibiotic streptomycin with similar antibacterial activity, was first synthesized in 1947 and subsequently used in the treatment of tuberculosis and gram-negative infections. Preparations for systemic use have been widely withdrawn as a result of concern regarding their severe ototoxicity. Dihydrostreptomycin is poorly absorbed from the gastrointestinal tract. It remains available in oral preparations in some countries.

Safety Profile

Poison by intravenous and intramuscular routes. Moderately toxic by subcutaneous and intraperitoneal routes. Human teratogenic effects by unspecified route: developmental abnormahties of the eye and ear. An experimental teratogen. Other experimental reproductive effects. Mutation data reported. A derivative of streptomycin; has anesthetic properties. When heated to decomposition it emits toxic fumes of NOx

Dihydrostreptomycin Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from Dihydrostreptomycin manufacturers

Dideu Industries Group Limited
Product
Dihydrostreptomycin 128-46-1
Price
US $1.10/g
Min. Order
1g
Purity
99.9%
Supply Ability
100 Tons Min
Release date
2021-06-22
Career Henan Chemical Co
Product
Dihydrostreptomycin 128-46-1
Price
US $1.00/g
Min. Order
1g
Purity
≥98%
Supply Ability
g/kg/Ton
Release date
2019-12-25

128-46-1, DihydrostreptomycinRelated Search:


  • DIHYDROSTREPTOMYCIN
  • Dihydrostreptomycin (base and/or unspecified salts)
  • 2-[(1S,3R,4S,5R,6R)-5-(Diaminomethylideneamino)-2-[(2R,3R,4R,5S)-3-[(2S,3S,4S,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-methylaminooxan-2-yl]oxy-4-hydroxy-4-(hydroxymethyl)-5-methyloxolan-2-yl]oxy-3,4,6-trihydroxycyclohexyl]guanidine
  • 2-[(1R,2R,3S,4R,5R,6S)-3-(diaminomethylideneamino)-4-[(2R,3R,4R,5S)-3-[(2S,3S,4S,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-(methylamino)oxan-2-yl]oxy-4-hydroxy-4-(hydroxymethyl)-5-methyloxolan-2-yl]oxy-2,5,6-trihydroxycyclohexyl]guanidine
  • Acetonitrile, 2-benzimidazolyl-
  • Benzimidazole, 2-cyanomethyl
  • 4-O-[2-O-[2-(Methylamino)-2-deoxy-α-L-glucopyranosyl]-5-deoxy-3-hydroxymethyl-α-L-lyxofuranosyl]-N,N'-bis(aminoiminomethyl)-D-streptamine
  • DHSM
  • DihydroestreptoMycin Sulfate
  • 2)-O-5-deoxy-3-C-(hydroxyMethyl)-a-L-lyxofuranosyl-(1&reg
  • 4)-N1,N3-bis(aMinoiMinoMethyl)-
  • D-StreptaMine,O-2-deoxy-2-(MethylaMino)-a-L-glucopyranosyl-(1&reg
  • dihydrostreptomycine sulphate
  • DihydrostreptomycineSulphateSterileUsp26
  • D-Streptamine, O-2-deoxy-2-(methylamino)-.alpha.-L-glucopyranosyl-(1?2)-O-5-deoxy-3-C-(hydroxymethyl)-.alpha.-L-lyxofuranosyl-(1?4)-N,N-bis(aminoiminomethyl)-
  • abiocine
  • dhms
  • dihydro-streptomyci
  • vibriomycin
  • D-Streptamine, O-2-deoxy-2-(methylamino)-α-L-glucopyranosyl-(1→2)-O-5-deoxy-3-C-(hydroxymethyl)-α-L-lyxofuranosyl-(1→4)-N1,N3-bis(aminoiminomethyl)-
  • Dihydrostreptomycin USP/EP/BP
  • 128-46-1
  • C21H41N7O12